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Genetic risk for bipolar disorder and schizophrenia predicts structure and function of the ventromedial prefrontal cortex

BACKGROUND: Bipolar disorder is highly heritable and polygenic. The polygenic risk for bipolar disorder overlaps with that of schizophrenia, and polygenic scores are normally distributed in the population. Bipolar disorder has been associated with structural brain abnormalities, but it is unknown ho...

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Autores principales: Abé, Christoph, Petrovic, Predrag, Ossler, William, Thompson, William H., Liberg, Benny, Song, Jie, Bergen, Sarah E., Sellgren, Carl M., Fransson, Peter, Ingvar, Martin, Landén, Mikael
Formato: Online Artículo Texto
Lenguaje:English
Publicado: CMA Joule Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8519489/
https://www.ncbi.nlm.nih.gov/pubmed/34291628
http://dx.doi.org/10.1503/jpn.200165
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author Abé, Christoph
Petrovic, Predrag
Ossler, William
Thompson, William H.
Liberg, Benny
Song, Jie
Bergen, Sarah E.
Sellgren, Carl M.
Fransson, Peter
Ingvar, Martin
Landén, Mikael
author_facet Abé, Christoph
Petrovic, Predrag
Ossler, William
Thompson, William H.
Liberg, Benny
Song, Jie
Bergen, Sarah E.
Sellgren, Carl M.
Fransson, Peter
Ingvar, Martin
Landén, Mikael
author_sort Abé, Christoph
collection PubMed
description BACKGROUND: Bipolar disorder is highly heritable and polygenic. The polygenic risk for bipolar disorder overlaps with that of schizophrenia, and polygenic scores are normally distributed in the population. Bipolar disorder has been associated with structural brain abnormalities, but it is unknown how these are linked to genetic risk factors for psychotic disorders. METHODS: We tested whether polygenic risk scores for bipolar disorder and schizophrenia predict structural brain alterations in 98 patients with bipolar disorder and 81 healthy controls. We derived brain cortical thickness, surface area and volume from structural MRI scans. In post-hoc analyses, we correlated polygenic risk with functional hub strength, derived from resting-state functional MRI and brain connectomics. RESULTS: Higher polygenic risk scores for both bipolar disorder and schizophrenia were associated with a thinner ventromedial prefrontal cortex (vmPFC). We found these associations in the combined group, and separately in patients and drug-naive controls. Polygenic risk for bipolar disorder was correlated with the functional hub strength of the vmPFC within the default mode network. LIMITATIONS: Polygenic risk is a cumulative measure of genomic burden. Detailed genetic mechanisms underlying brain alterations and their cognitive consequences still need to be determined. CONCLUSION: Our multimodal neuroimaging study linked genomic burden and brain endophenotype by demonstrating an association between polygenic risk scores for bipolar disorder and schizophrenia and the structure and function of the vmPFC. Our findings suggest that genetic factors might confer risk for psychotic disorders by influencing the integrity of the vmPFC, a brain region involved in self-referential processes and emotional regulation. Our study may also provide an imaging–genetics vulnerability marker that can be used to help identify individuals at risk for developing bipolar disorder.
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spelling pubmed-85194892021-10-17 Genetic risk for bipolar disorder and schizophrenia predicts structure and function of the ventromedial prefrontal cortex Abé, Christoph Petrovic, Predrag Ossler, William Thompson, William H. Liberg, Benny Song, Jie Bergen, Sarah E. Sellgren, Carl M. Fransson, Peter Ingvar, Martin Landén, Mikael J Psychiatry Neurosci Research Paper BACKGROUND: Bipolar disorder is highly heritable and polygenic. The polygenic risk for bipolar disorder overlaps with that of schizophrenia, and polygenic scores are normally distributed in the population. Bipolar disorder has been associated with structural brain abnormalities, but it is unknown how these are linked to genetic risk factors for psychotic disorders. METHODS: We tested whether polygenic risk scores for bipolar disorder and schizophrenia predict structural brain alterations in 98 patients with bipolar disorder and 81 healthy controls. We derived brain cortical thickness, surface area and volume from structural MRI scans. In post-hoc analyses, we correlated polygenic risk with functional hub strength, derived from resting-state functional MRI and brain connectomics. RESULTS: Higher polygenic risk scores for both bipolar disorder and schizophrenia were associated with a thinner ventromedial prefrontal cortex (vmPFC). We found these associations in the combined group, and separately in patients and drug-naive controls. Polygenic risk for bipolar disorder was correlated with the functional hub strength of the vmPFC within the default mode network. LIMITATIONS: Polygenic risk is a cumulative measure of genomic burden. Detailed genetic mechanisms underlying brain alterations and their cognitive consequences still need to be determined. CONCLUSION: Our multimodal neuroimaging study linked genomic burden and brain endophenotype by demonstrating an association between polygenic risk scores for bipolar disorder and schizophrenia and the structure and function of the vmPFC. Our findings suggest that genetic factors might confer risk for psychotic disorders by influencing the integrity of the vmPFC, a brain region involved in self-referential processes and emotional regulation. Our study may also provide an imaging–genetics vulnerability marker that can be used to help identify individuals at risk for developing bipolar disorder. CMA Joule Inc. 2021-07-22 /pmc/articles/PMC8519489/ /pubmed/34291628 http://dx.doi.org/10.1503/jpn.200165 Text en © 2021 CMA Joule Inc. or its licensors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an Open Access article distributed in accordance with the terms of the Creative Commons Attribution (CC BY-NC-ND 4.0) licence, which permits use, distribution and reproduction in any medium, provided that the original publication is properly cited, the use is noncommercial (i.e., research or educational use), and no modifications or adaptations are made. See: https://creativecommons.org/licenses/by-nc-nd/4.0/
spellingShingle Research Paper
Abé, Christoph
Petrovic, Predrag
Ossler, William
Thompson, William H.
Liberg, Benny
Song, Jie
Bergen, Sarah E.
Sellgren, Carl M.
Fransson, Peter
Ingvar, Martin
Landén, Mikael
Genetic risk for bipolar disorder and schizophrenia predicts structure and function of the ventromedial prefrontal cortex
title Genetic risk for bipolar disorder and schizophrenia predicts structure and function of the ventromedial prefrontal cortex
title_full Genetic risk for bipolar disorder and schizophrenia predicts structure and function of the ventromedial prefrontal cortex
title_fullStr Genetic risk for bipolar disorder and schizophrenia predicts structure and function of the ventromedial prefrontal cortex
title_full_unstemmed Genetic risk for bipolar disorder and schizophrenia predicts structure and function of the ventromedial prefrontal cortex
title_short Genetic risk for bipolar disorder and schizophrenia predicts structure and function of the ventromedial prefrontal cortex
title_sort genetic risk for bipolar disorder and schizophrenia predicts structure and function of the ventromedial prefrontal cortex
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8519489/
https://www.ncbi.nlm.nih.gov/pubmed/34291628
http://dx.doi.org/10.1503/jpn.200165
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